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PubPharm (391)
81
Design, synthesis and biological evaluation of 6-(nitroimidazole-1H-alkyloxyl)-4-anilinoquinazolines as efficient EGFR inhibitors exerting cytotoxic effects both under normoxia and hypoxia
enthalten in:
European journal of medicinal chemistry
| 2015
von
Cheng, W.
|
Zhu, S.
|
Ma, X.
| +4
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82
Design, synthesis and biological evaluation of novel 4-alkynyl-quinoline derivatives as PI3K/mTOR dual inhibitors
enthalten in:
European journal of medicinal chemistry
| 2015
von
Lv, X.
|
Ying, H.
|
Ma, X.
| +4
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83
Identification of novel 4-anilinoquinazoline derivatives as potent EGFR inhibitors both under normoxia and hypoxia
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Cheng, W.
|
Yuan, Y.
|
Qiu, N.
| +3
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84
Identification of novel 4-anilinoquinazoline derivatives as potent EGFR inhibitors both under normoxia and hypoxia
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Cheng, W.
|
Yuan, Y.
|
Qiu, N.
| +3
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85
Development of EGFR Family Small Molecule Inhibitors for Anticancer Intervention: An Overview of Approved Drugs and Clinical Candidates
enthalten in:
Current medicinal chemistry
| 2014
von
Cheng, W.
|
Hu, Y.
|
Sheng, R.
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86
Design, synthesis and biological evaluation of peptidyl epoxyketone proteasome inhibitors composed of β-amino acids
enthalten in:
Chemical biology & drug design
| 2014
von
Zhang, J.
|
Han, M.
|
Ma, X.
| +6
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87
Design and total synthesis of Mannich derivatives of marine natural product lamellarin D as cytotoxic agents
enthalten in:
European journal of medicinal chemistry
| 2014
von
Shen, L.
|
Xie, N.
|
Yang, B.
| +2
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88
Design and total synthesis of Mannich derivatives of marine natural product lamellarin D as cytotoxic agents
enthalten in:
European journal of medicinal chemistry
| 2014
von
Shen, L.
|
Xie, N.
|
Yang, B.
| +2
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89
Design, synthesis and biological evaluation of thienopyridinones as Chk1 inhibitors
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Song, P.
|
Peng, P.
|
Han, M.
| +5
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90
Design, synthesis and evaluation of rivastigmine and curcumin hybrids as site-activated multitarget-directed ligands for Alzheimer's disease therapy
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Li, Y.
|
Peng, P.
|
Tang, L.
| +3
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